1945-65-9 Usage
Uses
Used in Pharmaceutical Industry:
N,N-(4-xylylylide)bisaminoguanidine is used as a pharmaceutical compound for its potential therapeutic properties. The compound's unique structure allows it to interact with specific biological targets, making it a candidate for the development of new drugs.
Used in Chemical Research:
In the field of chemical research, N,N-(4-xylylylide)bisaminoguanidine serves as a valuable compound for studying the properties and reactivity of guanidine derivatives. Its unique structure can provide insights into the design and synthesis of new molecules with specific functions and applications.
Used in Material Science:
N,N-(4-xylylylide)bisaminoguanidine can be utilized in material science as a component in the development of novel materials with specific properties. Its chemical structure may contribute to the creation of materials with enhanced performance in areas such as conductivity, mechanical strength, or chemical stability.
Check Digit Verification of cas no
The CAS Registry Mumber 1945-65-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,4 and 5 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1945-65:
(6*1)+(5*9)+(4*4)+(3*5)+(2*6)+(1*5)=99
99 % 10 = 9
So 1945-65-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H14N8.2ClH/c11-9(12)17-15-5-7-1-2-8(4-3-7)6-16-18-10(13)14;;/h1-6H,(H4,11,12,17)(H4,13,14,18);2*1H/b15-5+,16-6+;;
1945-65-9Relevant academic research and scientific papers
Chen, Xijian,Dai, Xing,Xie, Rongzhen,Li, Jie,Khayambashi, Afshin,Xu, Lei,Yang, Chuang,Shen, Nannan,Wang, Yaxing,He, Linwei,Zhang, Yugang,Xiao, Chengliang,Chai, Zhifang,Wang, Shuao
, p. 1974 - 1977 (2020)
A new paradigm to remove toxic chromate anions from aqueous solution by crystallization of chromate-water clusters with imine-linked guanidinium cationic ligands is introduced. The guanidium-based cationic ligand was easily prepared through the imine cond
New furin inhibitors based on weakly basic amidinohydrazones
Sielaff, Frank,Than, Manuel E.,Bevec, Dorian,Lindberg, Iris,Steinmetzer, Torsten
body text, p. 836 - 840 (2011/02/27)
A novel series of amidinohydrazone-derived furin inhibitors was prepared; the most potent compounds 17 and 21 inhibit furin with Ki values of 0.46 and 0.59 μM, respectively. In contrast to inhibitor 17, which still contains a guanidino residue,
